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Tuesday, March 21, 2017

Volumetric modulated arc therapy

Introduction

Volumetric modulated arc therapy (VMAT) was first introduced in 2007 and described as a novel radiation technology designed to deliver treatment quickly and accurately. If appropriate for the treatment of cancer, it can reduce the number of patient visits and greatly improving recovery time. Volumetric Modulated Arc Therapy (VMAT) can be used for treating various types of cancer as prostate, head and neck tumors, as well as a range of other cancerous tumors (1).

All of them used data of Varian accelerators with its implementation of VMAT called RapidArc® (Varian Medical Systems, Inc., USA) and either prototypes of planning or optimizing systems or Varian’s Eclipse™. The ability to generate complex dose distributions is highly dependent on the optimization algorithm and capabilities of the delivery system used for treatment (2) [16, 17].
Image courtesy of Varian Medical Systems (3)
    Varian Rapid Arc
The main advantages of Volumetric Modulated Arc Therapy (VMAT) are precision and speed. Volumetric Modulated Arc Therapy (VMAT) focuses the radiation on the tumor while protecting healthy tissues (1). Each Volumetric Modulated Arc Therapy (VMAT) may reduce treatment times to as little as two minutes (3). Faster treatments improve the accuracy of radiation delivery, in addition to improving patient convenience and quality of life.
Volumetric Modulated Arc Therapy (VMAT) uses photons (W-rays) generated by a medical linear accelerator. The VMAT technique allows beam-on during a full gantry rotation of 360° with simultaneous modulation of the multileaf collimator (MLC) and a variation of gantry rotation speed as well as dose rate (4). Very small beams with varying intensities are aimed at a tumor and then rotated 360 degrees around the patient (4). This results in attacking the target in a complete 3D (three-dimensional) manner,  radiation therapist will be able to see the tumour during patient´s treatment and target it directly.
Volumetric Modulated Arc Therapy (VMAT) Treatment involves three basic steps: diagnosis, treatment planning, and treatment delivery. As part of the diagnosis, the medical team generates 3D diagnostic images (usually CT and/or PET) of the patient’s anatomy and then uses these images to specify the dose of radiation needed to treat the tumor (3). This article aims to discuss the current use of VMAT techniques in clinical process of radiation therapy that can be divided into as simulation and patient data acquisition, treatment planning and treatment delivery.

Simulation and patient data acquisition
The process of virtual simulation and data acquisition can be summarized in the following steps:
• Determination of the patient’s treatment position.
• Setting references on the patient’s skin.
• Acquisition of CT data and transfer to the virtual simulation workstation.
• Volume definition, which consists of delineation of target volumes (tumors) and of healthy surrounding structures (normal tissues and organs at risk).
• Determination of the treatment isocenter with respect to the references.
• Choice of plan parameters such as number of fields, energy, field size and orientation.
Modern treatment planning systems (TPSs) incorporate packages for virtual simulation. In consequence, it is possible to transfer the CT data to the TPS and carry out the volume definition, virtual simulation and treatment planning in a single integrated system. CT simulators offer important advantages over conventional simulators, allowing for complex and accurate treatment planning based on 3D data sets.
References
  1. M Teoh, CH Clark, K Wood, S Whitak, et.al. Volumetric modulated arc therapy: a review of current literature and clinical use in practice. Br J Radiol. 2011 Nov; 84(1007): 967–996.
  2. Palma DA, Verbakel WF, Otto K, Senan S: New developments in arc radiation therapy: a review. Cancer Treat Rev 2010, 36: 393-399
  3. Cleveland Clinic. Volumetric modulated arc therapy. Mars, 2017. http://my.clevelandclinic.org/health/articles/volumetric-modulated-arc-therapy
  4. Wolff D, Stieler F, Welzel G, Lorenz F, Abo-Madyan Y, et al. Volumetric modulated arc therapy (VMAT) vs. serial tomotherapy, step-and-shoot IMRT and 3D-conformal RT for treatment of prostate cancer. Radiother Oncol 2009, 93: 226-33.

Sunday, January 24, 2016

Cod liver oil intake and the risk of hypertensive disorder in pregnancy

A science paper is published at VJMP (Vietnam Journal of Medicine and Pharmacy) in 2015

http://vjmp.vn/noi-dung-tap-chi-3/fish-consumption-and-cod-liver-oil-intake-withthe-risk-of-hypertensive-disorders-in-pregnancy-337.htm

Fish consumption and cod liver oil intake withthe risk of hypertensive disorders in pregnancy

Thinh Tran Xuan1, Bryndis E. Birgisdottir1, Thorhallur I. Halldorsson1
Inga Thorsdottir1, Reynir T. Geirsson2
1Unit for Nutrition Research, Landspitali National University Hospital & Faculty of Human Nutrition, University of Iceland, 101 Reykjavik, Iceland.
2Department of Obsterics and Gynecology, Landspitali National University Hospital & Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland
ABSTRACT
Gestational hypertension and preeclampsia are common hypertensive disorders in pregnancy, associated with substantial morbidity and mortality for both mother and infants. A number of dietary factors have been related to hypertensive disorders in pregnancy. Fish consumption, fish liver oil supplements during pregnancy might be associated with gestational hypertension or preeclampsia.
Objectives
To examine the association between fish consumption and intake of cod liver oil with hypertensive disorders in pregnancy.
Methods
This retrospective cohort study was conducted at Landspitali National University Hospital, Reykjavik, Iceland in 1998. A total of 491 pregnant Icelandic women who gave birth at Landspitali National University Hospital in Reykjavik, aged 20-40, of normal weight before pregnancy were randomly selected from maternal records. Information on frequency of fish and cod liver oil consumption during pregnancy was collected from maternal records. We used gestational hypertension is defined as systolic blood pressure (SBP) ≥ 140 mmHg and/or a diastolic blood pressure (DBP) ≥ 90 mmHg as a primary outcome measure. Systolic and diastolic, isolated systolic, and isolated diastolic hypertension were used as secondary outcome measures.
Results
The prevalence of gestational hypertension and preeclampsia was 21% and 3%, respectively. Fish consumption was not associated with hypertensive disorders in pregnancy. Intake of fish liver oil was, however, positively associated with combined gestational hypertension (SBP) ≥ 140 and (DBP) ≥ 90. Using this definition women consuming one table spoon (≈ 9g) a day or more had an adjusted odds ratio of 6.3 (95% confidence interval: 2.2, 17.9) of having pregnancy hypertension compared to those with no intake. This association appeared to be driven by a relative shift from isolated diastolic hypertension to combined systolic and diastolic hypertension as overall fish liver oil was not associated with hypertension defined as (SBP) ≥ 140 and/or (DBP) ≥ 90.
Conclusions
No association was found between fish consumption and hypertensive disorders in pregnancy. Our results suggest that high (≈ 9 g/day) intake of fish liver oil may affect the severity of gestational hypertension. These findings are in line with previous reports from Iceland were high consumption of fish liver oil has been associated with hypertensive disorders in pregnancy.
Keywords
Fish, fish liver oil, n-3 PUFA, gestational hypertension, preeclampsia and hypertensive disorders in pregnancy.

Sunday, February 15, 2015

TheraSphere® (Yttrium-90) on Hepatocellular Carcinoma (HCC)


Introduction

TheraSphere® is Yttrium-90 microspheres radioembolization useful for liver cancer treatment and used generally to treat patients with hepatocellular carcinoma (HCC) and liver metastases (1).  In this paper, we become to discuss it, how to activate Yttrium-90 on the hepatocellular carcinoma, information of nuclide, radiation and the half-life. We also will analyze physiological features of Yttrium-90 on hepatocellular carcinoma cells and its side effects on the patient.

How to activate Yttrium-90 on hepatocellular carcinoma

TheraSphere (Yttrium-90 microspheres) are radioactive particles as a form of radiation treatment for unresectable HCC. TheraSphere is supplied in 0.5 mL of sterile, pyrogen-free water contained in a 0.3-mL V-bottom vial secured within a 12-mm clear acrylic vial shield. Yttrium-90 microspheres are administered by intra-arterial hepatic injection preferentially flow to tumor (Figure 1.), to patients with unresectable HCC who can have appropriately positioned hepatic arterial catheters (2).

           

Figure 1. Yttrium-90 microspheres are injected into the hepatic arteries preferentially flow to tumor (5).

The Yttrium-90 microspheres are trapped in tumors at the precapillary alveolar level. Patients can be released after infusion of the microspheres, since the Yttrium-90 decays only by beta-emission. Beta radiation is delivered internally to tumor at site of active growth. After administration, the bremsstrahlung radiation (electromagnetic radiation) is produced from the beta minus-interaction in the body, can be imaged and used to determine qualitative distribution in the liver (1).
A suspension of appropriately calibrated Yttrium-90 microspheres injected via the hepatic artery preferentially lodge in the peritumoral vessels, a process termed embolization, by which tumors are deprived of their nutrient arterial supply (3).

Information of nuclide, radiation and half-life

TheraSphere consists of nonbiodegradable glass microspheres (mean diameter of 25 μm) with yttrium-90 as an integral constituent of the glass. Yttrium-90 have the element´s atomic number (Z=39) and number of neutrons (N=51) and the atomic mass (A=90) (1).  Yttrium-90 is a pure beta emitted radionuclide, produced by neutron and decays to stable zirconium-90 with a physical half-life of 64.1 hours (2.67 days). The average energy of beta emission from the yttrium-90 is 0.9367 MeV, with a mean tissue penetration of 2.5 mm and a maximum of 10 mm (2).

One gigabecquerel (1GBq or 27mCi) delivers a total absorbed radiation dose of 50Gy/kg of tissue or per kilogram of targeted liver tissue provides a dose of 50Gy. In therapeutic use, in which the isotope decays to infinity, 94% of the radiation is delivered in 11 days (3).

Physiological Features of Yttrium-90 Microsphere

TheraSphere (MDS Nordion, Ottawa, Ontario, Canada) consists of millions of microscopic, radioactive glass Yttrium-90 microspheres (20–30 micrometers in diameter) with yttrium-90 as an integral constituent of the glass (3). The Yttrium-90 microspheres are not biodegradable; they decay only by a pure beta-emission, produced by neutron bombardment of Yttrium-90 in a reactor with a mean tissue penetration of 2.5 mm (2).

The Yttrium-90 microsphere is a high energy beta-emitter, would create a zone of radiation exposure confined to the vicinity of the tumor while maintaining nontumorous hepatic parenchymal exposure to tolerable levels. This forms the premise for radioembolization, also known as selective internal radiation therapy or microsphere brachytherapy (3). In clinical practice, millions of microspheres, measuring 30 micrometers in diameter incorporating yttrium-90, are injected via an intra-arterial catheter to the hepatic arterial supply of the tumor (3).

In patients with non-compromised liver function, the liver can tolerate 30 to 35Gy (1Gy represents the energy absorbed from ionizing radiation equal to 1 J/kg of tissue) when it is presented via uniform radiation fields with conventional fractionation (2).

Characteristics of yttrium-90 Microspheres are shown in table 1. as following (3, 4).

Table 1. Characteristics of Yttrium-90 Microsphere
Parameter
Glass
Trace name
ThereSphere® (MDS, Nordion, Canada)
Radioactive form
90Y (Yttrium-90)
Diameter
20-30 μm
Specific gravity
3.6 g/dL
Activity per particle
2500 Bq
Average number of  microspheres per administered activity
1.2-8 million
Material
Glass with Yttrium-90 in matrix
Liver tolerance radiation dose
30-35 Gy
FDA Approved
HCC
Recommended dose for liver tumor
2.0-3.0 GBq

           
           Yttrium-90 microspheres can be delivered in a local as segmental or sub-segmental, regional (lobar via the left or right hepatic artery), or whole-liver (via proper hepatic artery) manner, resulting in high radiation doses to arterial-fed tumors while sparing the liver parenchyma, which receives most of its blood supply from the portal vein. This method of radiation treatment provides a safety margin by distributing the radiation in a partial liver volume while treating tumors with tumoricidal doses of radiation. Yttrium-90 microsphere injection provides millions of scattered point sources of radioactivity, as opposed to the uniform fields of external beam radiotherapy. This difference in field properties for a given measure of radiation absorbed dose results in different biological effects (2).

The Side effects

Radioembolization is not without complications; it may lead to post-radioembolization syndrome which includes fatigue, nausea, vomiting, anorexia, fever, abdominal pain and cachexia. More serious adverse events include radiation induced liver toxicity, vascular injury when introducing the catheter, radiation pneumonitis from microspheres shunting around the liver and into the lungs, and gastrointestinal tract ulceration (4).

Absolute contraindications for the use of 90Y microspheres include pretreatment with 99mTc macroaggregated albumin scan demonstrating significant hepatopulmonary shunts, and inability to prevent deposition of the microspheres to the gastrointestinal tract with modern catheter techniques (4).

References

1.      Paul E. Christian, Kristen M. Waterstram. Nuclear Medicine and PET/CT: Technology and Techniques. 7thEd. Hardcover – March 18, 2011.

2.      Geschwind JF, Salem R, Carr BI, et al. Yttrium-90 Microspheres for the Treatment of     Hepatocellular Carcinoma. Gastroenterology. 2004 Nov;127(5 Suppl 1):194-205.

3.      Murthy R, Kamat P, Nuñez R, Salem R. Radioembolization of Yttrium-90 Microspheres for Hepatic Malignancy. Semin Intervent Radiol. 2008 Mar;25(1):48-57.

4.      Saad M Ibrahim, Robert J Lewandowski, Kent T Sato, et al. Radioembolization for the treatment of unresectable hepatocellular carcinoma: A clinical review. World J Gastroenterol. Mar 21, 2008; 14(11): 1664-1669.

5.      Figure is taken at. http://zoominmedical.com/cancer-tumor-diagram/

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Pulmonary Arterial Hypertensions in Infants


Sildenafil (viagra) in infants


Sildenafil in the treatment of pulmonary arterial hypertension in infants ...
.--------------------------------------------------------------------------------------------------------
.
Definition
------------
.
.
Pulmonary arterial hypertension(PAH) is a progressive, and often fatal, debilitating disorder.
The increased pulmonary artery pressure found in PAH is due to disturbances in key vascular mediator pathways including relative deficiencies of vasodilators such as nitric oxide (NO) and prostacyclin, as well as exaggerated production of vasoconstrictors such as endothelin and thromboxanes.
.
.
Symptoms
-------------
.
.
Progressive breathlessness, exertion limitation, frequent decline and failure of the right ventricle.
.
.
Mechanism of action of sildenafil
----------------------------------------
.
.
Sildenafil is a selective inhibitor of phosphodiesterase type 5 (PDE5). Present throughout the body, PDE5 is found in high concentrations in the lungs. Inhibition of PDE5 enhances the vasodilatory effects of nitric oxide in pulmonary hypertension by preventing the degradation of cyclic guanosine monophosphate (cGMP), which promotes relaxation of vascular smooth muscle and increases blood flow. In animal models and human trials, sildenafil has been found to produce a relatively selective reduction in pulmonary artery pressure without adverse systemic hemodynamic effects after 3 months of oral therapy. Inhibition of PDE5 by sildenafil may also enhance the platelet antiaggregatory activity of nitric oxide and inhibit thrombus formation.
.
.
Infant’s dose
----------------
.
.
The protocol for dosing was
.
(1) first dose of 1 mg/kg/dose within 30 minutes admission or within 12 hours of delivery (whichever earlier),
(2) Dosing every six hours for a maximum of 8 doses,
(3) Dose was doubled if the oxygenation index (OI) or SpO2 did not improve (If OI continued to be <10% of previous value and SpO2 was not increasing >5 of previous value) and blood pressure remained stable.

Definition

Pulmonary arterial hypertension(PAH) is a progressive, and often fatal, debilitating disorder.

 The increased pulmonary artery pressure found in PAH is due to disturbances in key vascular mediator pathways including relative deficiencies of vasodilators such as nitric oxide (NO) and prostacyclin, as well as exaggerated production of vasoconstrictors such as endothelin and thromboxanes.

Symptoms

Progressive breathlessness, exertion limitation, frequent decline and failure of the right ventricle.

Mechanism of action of sildenafil

Sildenafil is a selective inhibitor of phosphodiesterase type 5 (PDE5). Present throughout the body, PDE5 is found in high concentrations in the lungs. Inhibition of PDE5 enhances the vasodilatory effects of nitric oxide in pulmonary hypertension by preventing the degradation of cyclic guanosine monophosphate (cGMP), which promotes relaxation of vascular smooth muscle and increases blood flow. In animal models and human trials, sildenafil has been found to produce a relatively selective reduction in pulmonary artery pressure without adverse systemic hemodynamic effects after 3 months of oral therapy. Inhibition of PDE5 by sildenafil may also enhance the platelet antiaggregatory activity of nitric oxide and inhibit thrombus formation.

Infant’s dose

The protocol for dosing was

(1) first dose of 1 mg/kg/dose within 30 minutes admission or within 12 hours of delivery (whichever earlier),

 (2) Dosing every six hours for a maximum of 8 doses,

 (3) Dose was doubled if the oxygenation index (OI) or SpO2 did not improve (If OI continued to be <10% of previous value and SpO2 was not increasing >5 of previous value) and blood pressure remained stable.

 
 how can i prepare the infant's dose from viagra tablet???

  newborns received oral Sildenafil solution through feeding tube which was prepared by crushing a 50 mg tablet of sildenafil in distilled water or simple syrup to make a concentration of 5 mg/ml.

notes

At 2012The U.S.Food and DrugAdministration (FDA) is recommending that sildenafil not be prescribed to children (ages 1 through 17) for pulmonary arterial hypertension. This recommendation against use is based on a recent long-term clinical pediatric trial showing that: (1) children taking a high dose of sildenafil had a higher risk of death than children taking a low dose and (2) the low doses of sildenafil are not effective in improving exercise ability.

 

References

1)      Clavecilla SQ. New insights into the treatment of pulmonary arterial hypertension. Formulary, 2003 Mar; 38(3): 150-4, 157-8, 160.

2) Mehta S. Sildenafil for pulmonary arterial hypertension: exciting, but protection required. Chest. 2003 Apr; 123(4): 989-92.

3) Pfizer Inc. FDA Approves Pfizer’s Revatio as Treatment for Pulmonary Arterial Hypertension.http://www.pfizer.com/pfizer/are/news_releases/2005pr/mn_2005_0606.jsp#additional. Accessed June 23, 2005.

4) Kataoka M, Satoh T, Manabe T, Anzai T, Yoshikawa T, Mitamura H, Ogawa S. Oral sildenafil improves primary pulmonary hypertension refractory to epoprostenol. Circ J. 2005 Apr;69(4):461-5.

5) Kanthapillai P, Lasserson T, Walters E. Sildenafil for pulmonary hypertension. Cochrane Database Syst Rev. 2004 Oct 18;(4):CD003562.

6) Karatza AA, Bush A, Magee AG. Safety and efficacy of Sildenafil therapy in children with pulmonary hypertension. Int J Cardiol. 2005 Apr 20;100(2):267-73.

7) Leuchte HH, et al. Hemodynamic response to sildenafil, nitric oxide, and iloprost in primary pulmonary hypertension. Chest. 2004 Feb; 125(2): 580-6.

8) Chockalingam A, Gnanavelu G, Venkatesan S, Elangovan S, Jagannathan V, Subramaniam T, Alagesan R, Dorairajan S. Efficacy and optimal dose of sildenafil in primary pulmonary hypertension. Int J Cardiol. 2005 Mar 10;99(1):91-5.

9) Lee AJ, Chiao TB, Tsang MP. Sildenafil for pulmonary hypertension. Ann Pharmacother. 2005 May;39(5):869-84.

10) Sastry BK. Clinical efficacy of sildenafil in primary pulmonary hypertension: a randomized, placebo-controlled, double-blind, crossoverstudyImage. J Am Coll Cardiol, 2004 Apr;43 (7), pp. 1149-53.

11) Ng J, Finney SJ, Shulman R, Bellingan GJ, Singer M, Glynne PA. Treatment of pulmonary hypertension in the general adult intensive care unit: a role for oral sildenafil? Br J Anaesth. 2005 Jun;94(6):774-7.

12) American Heart Association rapid access journal report. Impotence drug may help children with fatal lung disorder. 06/23/2005.http://www.americanheart.org/presenter.jhtml?identifier=3031499. Accessed: June 23, 2005.

 National Heart, Lung, and Blood Institute: "What Is Pulmonary Arterial Hypertension?" National Heart, Lung, and Blood Institute: "Living with Pulmonary Arterial Hypertension." WebMD Medical News:"Viagra Label May Note Rare Vision Problems. “ViagraThe Associated Press.

Links

















 

Check here all the unusual uses for viagra

https://www.facebook.com/photo.php?fbid=320947854736100&set=a.308153912682161.1073741828.100004626645250&type=1 .
.
how can i prepare the infant's dose from viagra tablet???
------------------------------------------------------------------------
newborns received oral Sildenafil solution through feeding tube which was prepared by crushing a 50 mg tablet of sildenafil in distilled water or simple syrup to make a concentration of 5 mg/ml.
.
.
.
notes
-------
.
.
At 2012The U.S.Food and DrugAdministration (FDA) is recommending that sildenafil not be prescribed to children (ages 1 through 17) for pulmonary arterial hypertension. This recommendation against use is based on a recent long-term clinical pediatric trial showing that: (1) children taking a high dose of sildenafil had a higher risk of death than children taking a low dose and (2) the low doses of sildenafil are not effective in improving exercise ability.
.
.
References
---------------
Clavecilla SQ. New insights into the treatment of pulmonary arterial hypertension. Formulary, 2003 Mar; 38(3): 150-4, 157-8, 160.

2) Mehta S. Sildenafil for pulmonary arterial hypertension: exciting, but protection required. Chest. 2003 Apr; 123(4): 989-92.

3) Pfizer Inc. FDA Approves Pfizer’s Revatio as Treatment for Pulmonary Arterial Hypertension.http://www.pfizer.com/pfizer/are/news_releases/2005pr/mn_2005_0606.jsp#additional. Accessed June 23, 2005.

4) Kataoka M, Satoh T, Manabe T, Anzai T, Yoshikawa T, Mitamura H, Ogawa S. Oral sildenafil improves primary pulmonary hypertension refractory to epoprostenol. Circ J. 2005 Apr;69(4):461-5.

5) Kanthapillai P, Lasserson T, Walters E. Sildenafil for pulmonary hypertension. Cochrane Database Syst Rev. 2004 Oct 18;(4):CD003562.

6) Karatza AA, Bush A, Magee AG. Safety and efficacy of Sildenafil therapy in children with pulmonary hypertension. Int J Cardiol. 2005 Apr 20;100(2):267-73.

7) Leuchte HH, et al. Hemodynamic response to sildenafil, nitric oxide, and iloprost in primary pulmonary hypertension. Chest. 2004 Feb; 125(2): 580-6.

8) Chockalingam A, Gnanavelu G, Venkatesan S, Elangovan S, Jagannathan V, Subramaniam T, Alagesan R, Dorairajan S. Efficacy and optimal dose of sildenafil in primary pulmonary hypertension. Int J Cardiol. 2005 Mar 10;99(1):91-5.

9) Lee AJ, Chiao TB, Tsang MP. Sildenafil for pulmonary hypertension. Ann Pharmacother. 2005 May;39(5):869-84.

10) Sastry BK. Clinical efficacy of sildenafil in primary pulmonary hypertension: a randomized, placebo-controlled, double-blind, crossoverstudyImage. J Am Coll Cardiol, 2004 Apr;43 (7), pp. 1149-53.

11) Ng J, Finney SJ, Shulman R, Bellingan GJ, Singer M, Glynne PA. Treatment of pulmonary hypertension in the general adult intensive care unit: a role for oral sildenafil? Br J Anaesth. 2005 Jun;94(6):774-7.

12) American Heart Association rapid access journal report. Impotence drug may help children with fatal lung disorder. 06/23/2005.http://www.americanheart.org/presenter.jhtml?identifier=3031499. Accessed: June 23, 2005.
National Heart, Lung, and Blood Institute: "What Is Pulmonary Arterial Hypertension?" National Heart, Lung, and Blood Institute: "Living with Pulmonary Arterial Hypertension." WebMD Medical News:"Viagra Label May Note Rare Vision Problems. “ViagraThe Associated Press.
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Links
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